|
HS Code |
773707 |
| Chemical Name | 2-Bromo-6-Fluorophenol |
| Molecular Formula | C6H4BrFO |
| Molecular Weight | 191.0 g/mol |
| Cas Number | 351003-92-6 |
| Appearance | White to off-white solid |
| Melting Point | 65-68°C |
| Purity | Typically ≥97% |
| Smiles | C1=CC(=C(C(=C1)F)O)Br |
| Inchi | InChI=1S/C6H4BrFO/c7-4-2-1-3-5(8)6(4)9/h1-3,9H |
| Solubility | Slightly soluble in water, soluble in organic solvents |
As an accredited 2-Bromo-6-Fluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Bromo-6-Fluorophenol, securely sealed with a screw cap and clear hazard labeling. |
| Shipping | 2-Bromo-6-Fluorophenol is shipped in tightly sealed containers to prevent moisture or contamination, typically as a solid. It is packaged according to hazardous material guidelines due to its chemical properties. Shipping complies with local and international regulations, ensuring safe handling, labeling, and transport to minimize risk during transit. |
| Storage | 2-Bromo-6-Fluorophenol should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, dry, and well-ventilated area. Store away from sources of ignition, incompatible substances such as strong oxidizers, and acids. Ensure the storage area is clearly labeled and designed to prevent contamination and environmental release. Handle using appropriate personal protective equipment. |
Competitive 2-Bromo-6-Fluorophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Anyone who spends time on the chemical production line knows there’s a unique pride in seeing your material serve as the building block of more advanced molecules. 2-Bromo-6-Fluorophenol shows up regularly on our batch planning boards for a reason—it isn’t just another halogenated phenol. Its potential rests in its dual substitution, offering a chemical backbone both reactive and selective in modern synthesis. The bromo and fluoro groups on the phenolic ring create opportunities for coupling, crosslinking, or fine-tuning downstream pharmacophores. The phenol group itself offers a reliable anchor point for further derivatization, and the unique substitution pattern doesn’t just appear by accident; it requires careful, tuned production steps, especially when scaling beyond a few kilograms.
From the perspective of a producer, differentiation starts even before the raw materials enter the warehouse. Each edition of 2-Bromo-6-Fluorophenol we manufacture, using CAS number 395-18-8, demands tight control over our bromination and fluorination routes. Modern pharmaceutical and agrochemical research increasingly seeks halogenated intermediates with very specific substitution patterns. Impurities, no matter how minor they may seem in a lab notebook, create downstream headaches—so production isn’t a matter of brute-force chemistry; it calls for both an experienced eye and diligence during purification.
Our batches most often target a purity of 98% or higher, with color and moisture inspected in every lot. Moisture often escapes casual review, yet trace water changes solubility, influences crystallization, and at scale can throw off otherwise repeatable synthesis steps. We use glass-lined reactors that stand up to both hydrobromic and hydrofluoric acid, along with corrosion-resistant transfer lines that let us switch between solvents without leaching. Over years, we’ve refined our distillation and recrystallization schedules to pull the product free of polyhalogenated and hydroxy byproducts. Granular powder or crystalline forms sometimes suit different labs—pharmaceutical researchers demand an off-white solid with low trace metal content, while other sectors want packed powders that move easily in bulk.
2-Bromo-6-Fluorophenol isn’t an end in itself; it’s a stepping-stone in growing pharmaceutical actives, crop protection products, and specialty materials. Contract clients regularly request this intermediate for Suzuki couplings, etherification, or nucleophilic aromatic substitution. Each transformation relies on the clean selectivity the bromo and fluoro groups afford. Compared to its close cousin 2-Bromo-4-Fluorophenol, the 6-fluoro isomer reacts differently in couplings, giving distinct regioselective advantages during route scouting for drug or pigment synthesis.
From the factory level up, we’ve learned not to cut corners in the drying stage. Aromatic fluorophenols can scavenge atmospheric moisture, so we employ vacuum-drying and nitrogen-packed storage to shield quality from seasonal humidity swings. This extends shelf life and gives downstream chemists a more predictable starting point in their syntheses.
Any producer who’s fielded a late-night call from a process chemist with a stalled reaction knows the value of traceability. Each batch of 2-Bromo-6-Fluorophenol moves through our dedicated QC labs for NMR, GC-MS, and HPLC analysis. Years in the specialty chemical sector taught us to keep spectral data for every lot in secure archives. When a customer’s reaction profile shifts, having full impurity maps and production records can mean the difference between a quick root-cause analysis and days of backtracking.
Contaminants like polyhalogenated congeners may not register during single-gram syntheses, but extra unreacted fluorobenzene cropping up in an industrial run will affect yields and even regulatory acceptability. Our onsite analytics team works shoulder-to-shoulder with plant operators; we catch excess byproducts at the mother liquor stage, not after full-scale isolation. It saves material, minimizes downtime, and supports transparent communication with R&D teams looking for root causes in their own processes.
Daily plant operations bring a sharp awareness that halogenated organics require not just precision, but also respect for environmental boundaries. We operate solvent recovery loops to minimize emission of aromatics and halides. Our liquid waste neutralization feeds into a multi-stage treatment train, designed to break down residual organics and scavenge heavy metals. Internal audits make us continually re-examine the solvents and starting materials we source, updating to less hazardous alternatives where feasible. These measures aren’t just regulatory box-ticking—they shape the decisions we make on process routes and influence the claims we can offer when buyers seek documentation for sustainable procurement.
Some customers voice concern about the sustainability of using so many brominated and fluorinated intermediates. Their questions are valid. We’ve responded by developing recycling schemes for spent bromide and fluoride, returning them as much as possible to our supply stream or to specialized reclamation projects elsewhere. Transparency with supply chain partners about halogen source, waste management, and environmental release also reassures technical buying teams under increasing compliance scrutiny.
Every innovation in the chemical sector starts with feedback from suppliers and customers willing to share their pain points. Over the years, a steady dialogue with clients has prompted us to offer 2-Bromo-6-Fluorophenol in both small laboratory vials and multi-kilogram PE drums, along with more flexible packaging for pilot projects. Customers in medicinal chemistry often request batches with purity sharing full chromatographic profiles. Others want a specific sieve fraction or custom homogenization for automated handling in larger reactors.
We also keep an eye on evolving application fields. With the rise of new materials—OLEDs, specialty polymers, and photoinitiators—halogenated aromatic intermediates like ours now play roles well beyond pharmaceuticals. Each new project proposal turns into a technical exercise: Are our current impurity specs tight enough for excimer laser applications? Will a custom particle size distribution improve dissolution in a client’s resin matrix? Will improved color grade offer better outcomes in pigment intermediates?
Internal process adaptation has become part of our routine; we frequently run joint investigations with customer labs. For process development support, we often send technical liaisons to customer sites, helping troubleshoot scale-up—translating batch results from bench top to plant, not just handing over a COA.
Those who’ve handled multi-ton volumes of various mono- and di-halogenated phenols know nuances matter. Substituent position isn’t a trivial detail—electronic effects govern subsequent reactivity and even pharmacokinetic profiles downstream. 2-Bromo-6-Fluorophenol distinguishes itself from, say, 2-Bromo-4-Fluorophenol or 4-Bromo-2-Fluorophenol with different activation profiles in cross-coupling protocols. The 2 and 6 positions in our product ring-fence the phenol group and tune acidity, which allows for unique selectivity when further derivatizing under basic or metal-catalyzed conditions.
2-Bromo-6-Fluorophenol often gets chosen over its isomers for routes aiming to avoid para-substitution, where side-reactions are more prevalent. This selectivity expedites process development, especially in medicinal chemistry or in multi-step, convergent syntheses common to late-stage drug or pigment research. Our experience confirms labs pay a premium for the consistency in substitution, maintaining tight tolerances on regio-isomer contamination.
Compared with the parent phenol or simple brominated or fluorinated analogs, our compound wields distinct reactivity in both nucleophilic aromatic substitution and palladium-catalyzed transformations. The synergy between bromine and fluorine in the ortho positions suppresses some degradative reactions under heat, improving yields and lowering byproduct loads. These practical differences, gleaned from years of batch and kilo-lab experience, drive preference for this intermediate across multiple sectors.
Experienced producers crack the code of aromatic halogenation through a mix of patience and iteration. Some hires with years of lab background often remark on the difference in real-world scaling—temperature gradients and impurity profiles that don’t show up under ideal university lab conditions. We keep teams cross-trained between kitting, production, and QA so that every process handshake, from charging the reactor to packing the final drum, falls under direct oversight.
Demand for halogenated intermediates is showing no sign of slowing. Pharmaceutical and crop science R&D both demand relay points like 2-Bromo-6-Fluorophenol for divergent synthetic explorations. Researchers venturing into new kinase inhibitor classes, for instance, lean on the selectivity this molecule offers in their palladium-catalyzed transformations. In advanced material contexts, such as OLED or specialty resin design, the presence of both bromine and fluorine in the molecule opens up tuning opportunities that single-halogenated compounds cannot match.
We strive for staff continuity and hands-on learning—newer team members often shadow experienced operators through the entire batch. Seasoned technicians know, often by smell and appearance, the signs that a run is progressing as expected or drifting off-spec. Our approach rewards familiarity, and troubleshooting skills go hand-in-hand with a sense of ownership.
One of the most gratifying aspects of making 2-Bromo-6-Fluorophenol lies in watching customers bring new products to market powered by our intermediate. We receive regular feedback on how process impurities, packaging adaptations, or changes in microstructure directly affect client outcomes. Our technical team leverages this data to continually enhance batch reproducibility, tailor drying times to customer feedback, and share best practices on storage and handling.
Each year lands new legislation about halogen content, trace impurity tolerance, or controlled substance lists. Staying in front of shifting regulatory and technical trends comes from collaboration—not just inside the company but across the network of customers we serve and suppliers we work with. This approach has led us to continually update our own analytical techniques, increasing the resolution of our GC-MS and NMR archives which improves customer trust.
Plant managers, chemists, and logistics staff alike face headwinds: unpredictable raw material shortages, evolving customer requirements, rising sustainability bar, and the technical challenge of scaling intricate molecules. The lesson of years in production has taught us to view each challenge as an opportunity for improvement. By optimizing waste neutralization systems and maximizing solvent reclamation, we address environmental concerns. By investing in detailed batch analytics and technical support, we proactively reduce quality concerns—offering real solutions when customers demand evidence of both safety and performance.
Producers like us stay flexible—ready to tweak a reaction path, adapt a purification sequence, or adjust an analytical method when a customer’s data highlight a need. Our investment in staff training and equipment means that as new application spaces open—be it in next-generation pharmaceuticals or optoelectronic materials—we already have the experience base to supply high-quality 2-Bromo-6-Fluorophenol in ways customers recognize and appreciate.
Direct production experience builds not just product, but reputation. In halogenated intermediate markets, relationships hinge on consistent supply and open channels for technical feedback. Each batch of 2-Bromo-6-Fluorophenol we produce underpins processes across the globe, often as the invisible foundation for high-value molecules that drive advances in science, agriculture, and design.
Our team approaches each new lot not as a routine exercise, but as an opportunity to raise standards, solve emerging technical challenges, and support the innovators who trust our inputs. The cycle of learning and upgrading continues, powered by close collaboration with those at the front lines of synthesis and manufacturing. For every flask drawn from our drums, there’s a chain of careful decisions and hard-won knowledge built in. That’s the perspective only a genuine manufacturer brings to the intricate, ever-expanding world of chemical intermediates.